Detalhe da pesquisa
1.
Congenital fibrinogen disorders: Strengthening genotype-phenotype correlations through novel genetic diagnostic tools.
Br J Haematol
; 203(3): 355-368, 2023 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-37583269
2.
Inhibition of retinoic acid signaling impairs cranial and spinal neural tube closure in mice lacking the Grainyhead-like 3 transcription factor.
Biochem Biophys Res Commun
; 635: 244-251, 2022 12 20.
Artigo
Inglês
| MEDLINE | ID: mdl-36283337
3.
Neomorphic effects of the neonatal anemia (Nan-Eklf) mutation contribute to deficits throughout development.
Development
; 144(3): 430-440, 2017 02 01.
Artigo
Inglês
| MEDLINE | ID: mdl-28143845
4.
Self-repopulating recipient bone marrow resident macrophages promote long-term hematopoietic stem cell engraftment.
Blood
; 132(7): 735-749, 2018 08 16.
Artigo
Inglês
| MEDLINE | ID: mdl-29945953
5.
Corrupted DNA-binding specificity and ectopic transcription underpin dominant neomorphic mutations in KLF/SP transcription factors.
BMC Genomics
; 20(1): 417, 2019 May 24.
Artigo
Inglês
| MEDLINE | ID: mdl-31126231
6.
Variants leading to dysfibrinogenaemia in the fibrinogen α-chain at residue Arg19 are not solely associated with bleeding, but also with thrombotic events-RESPONSE.
Br J Haematol
; 2024 Apr 12.
Artigo
Inglês
| MEDLINE | ID: mdl-38607668
7.
Recommendations for the use of pegylated interferon-α in the treatment of classical myeloproliferative neoplasms.
Intern Med J
; 49(8): 948-954, 2019 08.
Artigo
Inglês
| MEDLINE | ID: mdl-30411442
8.
Krüppel-like factors compete for promoters and enhancers to fine-tune transcription.
Nucleic Acids Res
; 45(11): 6572-6588, 2017 Jun 20.
Artigo
Inglês
| MEDLINE | ID: mdl-28541545
9.
Promiscuous DNA-binding of a mutant zinc finger protein corrupts the transcriptome and diminishes cell viability.
Nucleic Acids Res
; 45(3): 1130-1143, 2017 02 17.
Artigo
Inglês
| MEDLINE | ID: mdl-28180284
10.
Investigation of the variable In(Lu) phenotype caused by KLF1 variants.
Transfusion
; 58(10): 2414-2420, 2018 10.
Artigo
Inglês
| MEDLINE | ID: mdl-30222867
11.
KLF1-null neonates display hydrops fetalis and a deranged erythroid transcriptome.
Blood
; 125(15): 2405-17, 2015 Apr 09.
Artigo
Inglês
| MEDLINE | ID: mdl-25724378
12.
A case-based discussion of clinical problems in the management of patients treated with ruxolitinib for myelofibrosis.
Intern Med J
; 47(3): 262-268, 2017 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-28260257
13.
Fibroblast growth factor-1 (FGF-1) promotes adipogenesis by downregulation of carboxypeptidase A4 (CPA4) - a negative regulator of adipogenesis implicated in the modulation of local and systemic insulin sensitivity.
Growth Factors
; 34(5-6): 210-216, 2016 12.
Artigo
Inglês
| MEDLINE | ID: mdl-28209092
14.
The F-BAR protein NOSTRIN participates in FGF signal transduction and vascular development.
EMBO J
; 31(15): 3309-22, 2012 Aug 01.
Artigo
Inglês
| MEDLINE | ID: mdl-22751148
15.
Interaction of c-Myb with p300 is required for the induction of acute myeloid leukemia (AML) by human AML oncogenes.
Blood
; 123(17): 2682-90, 2014 Apr 24.
Artigo
Inglês
| MEDLINE | ID: mdl-24596419
16.
Congenital Anemia Phenotypes Due to KLF1 Mutations.
J Pediatr Hematol Oncol
; 43(1): e148-e149, 2021 01.
Artigo
Inglês
| MEDLINE | ID: mdl-32815883
17.
Identification of novel hypomorphic and null mutations in Klf1 derived from a genetic screen for modifiers of α-globin transgene variegation.
Genomics
; 105(2): 116-22, 2015 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-25451176
18.
Macrophages and regulation of erythropoiesis.
Curr Opin Hematol
; 22(3): 212-9, 2015 May.
Artigo
Inglês
| MEDLINE | ID: mdl-25693142
19.
Novel roles for KLF1 in erythropoiesis revealed by mRNA-seq.
Genome Res
; 22(12): 2385-98, 2012 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-22835905
20.
Clinical acceleration of JAK2 p.V617F driven myeloproliferative disease due to a new uncommon homozygous MPL p.Y591D mutation.
Haematologica
; 105(8): e428-e431, 2020 08.
Artigo
Inglês
| MEDLINE | ID: mdl-32499240